Heterostructure Cu3P−Ni2P/CP catalyst assembled membrane electrode for high-efficiency electrocatalytic nitrate to ammonia

被引:0
|
作者
Meng Jin
Jiafang Liu
Xian Zhang
Shengbo Zhang
Wenyi Li
Dianding Sun
Yunxia Zhang
Guozhong Wang
Haimin Zhang
机构
[1] Chinese Academy of Sciences,Laboratory of Materials Physics, Centre for Environmental and Energy Nanomaterials, Anhui Key Laboratory of Nanomaterials and Nanotechnology, CAS Center for Excellence in Nanoscience, Institute of Solid State Physics, Hefei Inst
[2] University of Science and Technology of China,undefined
[3] Anhui Contango New Energy Technology Co.,undefined
[4] Ltd.,undefined
来源
Nano Research | 2024年 / 17卷
关键词
electrocatalytic nitrate reduction to ammonia; three-type reactors; membrane-electrode-assemblies system; operando ATR-IRRAS; successive hydrodeoxygenation pathway;
D O I
暂无
中图分类号
学科分类号
摘要
Electrochemical nitrate reduction reaction (NO3RR) is a promising means for generating the energy carrier ammonia. Herein, we report the synthesis of heterostructure copper-nickel phosphide electrocatalysts via a simple vapor-phase hydrothermal method. The resultant catalysts were evaluated for electrocatalytic nitrate reduction to ammonia (NH3) in three-type electrochemical reactors. In detail, the regulation mechanism of the heterogeneous Cu3P−Ni2P/CP−x for NO3RR performance was systematically studied through the H-type cell, rotating disk electrode setup, and membrane-electrode-assemblies (MEA) electrolyzer. As a result, the Cu3P−Ni2P/CP−0.5 displays the practicability in an MEA system with an anion exchange membrane, affording the largest ammonia yield rate (RNH3) of 1.9 mmol·h−1·cm−2, exceeding most of the electrocatalytic nitrate reduction electrocatalysts reported to date. The theoretical calculations and in-situ spectroscopy characterizations uncover that the formed heterointerface in Cu3P−Ni2P/CP is beneficial for promoting nitrate adsorption, activation, and conversion to ammonia through the successive hydrodeoxygenation pathway.
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页码:4872 / 4881
页数:9
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